Back to search

Article

Redefining counting of copy number variations and single-nucleotide polymorphisms by applying a novel concept based on the STexS and STexS II method

2023-09-26

Abstract excerpt

<title>Abstract</title> <p>Human genes exist as numerous copy number variations (CNV) and single-nucleotide polymorphisms (SNP) that exert control over the majority of the bodies’ core functions. On average, 12–16% of human genes have CNVs and a single gene can have anywhere from a few hundred to several thousand SNPs. By virtue of numerous genome-wide association studies (GWAS), we now know that CNVs and SNPs ca...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
b81f4010-2013-57d0-8b2e-af2203ad30c7
DOI
10.21203/rs.3.rs-3353838/v1
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Redefining counting of copy number variations and single-nucleotide polymorphisms by applying a novel concept based on the STexS and STexS II methodDOI 10.21203/rs.3.rs-3353838/v1
Select a neighboring publication to make it the new centre.